HCID 20541907, compound → HCID 20542017, compound

HRID 1863476Notes

Reaction equation

HRID 1863476 reaction equation
C1O[CH:4]([CH:5]2[CH2:14][CH2:13][C:12]3[C:7](=[C:8]([O:17][CH3:18])[CH:9]=[C:10]([O:15][CH3:16])[CH:11]=3)[C:6]2=O)[O:3]C1.COC1C=C2C(=C(OC)C=1)C=C(C=O)C=C2>>[CH3:16][O:15][C:10]1[CH:11]=[C:12]2[C:7](=[C:8]([O:17][CH3:18])[CH:9]=1)[CH:6]=[C:5]([CH2:4][OH:3])[CH:14]=[CH:13]2

Participants

3

Reactant 2

HCID 20541907HCID 20541907, compoundHCID 20542010HCID 20542010, compound

Product 1

HCID 20542017HCID 20542017, compound

Procedure

Following a procedure similar to that described in Example 155 but substituting for 1,2,3,4-tetrahydro-6,8-dimethoxy-1-oxo-2-naphthaldehyde ethylene acetal an equivalent amount of 6,8-dimethoxy-2-naphthaldehyde, there is obtained 6,8-dimethoxy-2-naphthalenemethanol.

Sources & evidence

ORD record
ord-ddad0548f9744c4f9f7f23ca3eb4e8ad
Source dataset
uspto-grants-1979_09
Patent number
US04169108

Reaction notes

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